Olupot-Olupot Peter, Aloroker Florence, Mpoya Ayub, Mnjalla Hellen, Paasi George, Nakuya Margaret, Houston Kirsty, Obonyo Nchafatso, Hamaluba Mainga, Evans Jennifer A, Dewez Manuel, Atti Salifou, Guindo Ousmane, Ouattara San Maurice, Chara Abdullahi, Sainna Hadiza Alhaji, Amos Omokore Oluseyi, Ogundipe Oluwakemi, Sunyoto Temmy, Coldiron Matthew, Langendorf Celine, Scherrer Marie-Francoise, Petrucci Roberta, Connon Roisin, George Elizabeth C, Gibb Diana M, Maitland Kathryn
Department of Paediatrics, Mbale Clinical Research Institute, Pallisa Road, Mbale, PO Box 291, Uganda.
Mbale Regional Referral Hospital, Pallisa Road, Mbale, PO Box 291, Uganda.
Wellcome Open Res. 2024 Jan 16;6:160. doi: 10.12688/wellcomeopenres.16885.2. eCollection 2021.
Children hospitalised with severe acute malnutrition (SAM) are frequently complicated (>50%) by diarrhoea ( ≥3 watery stools/day) which is accompanied by poor outcomes. Rehydration guidelines for SAM are exceptionally conservative and controversial, based upon expert opinion. The guidelines only permit use of intravenous fluids for cases with advanced shock and exclusive use of low sodium intravenous and oral rehydration solutions (ORS) for fear of fluid and/or sodium overload. Children managed in accordance to these guidelines have a very high mortality. The proposed GASTROSAM trial will reappraise current recommendations with mortality as the primary outcome. We hypothesize that liberal rehydration strategies for both intravenous and oral rehydration in SAM children with diarrhoea may reduce adverse outcomes.
An open Phase II trial, with a partial factorial design, enrolling children in Uganda, Kenya, Nigeria and Niger aged 6 months to 12 years with SAM hospitalised with gastroenteritis (>3 loose stools/day) and signs of moderate and severe dehydration. In Stratum A (severe dehydration) children will be randomised (1:1:2) to WHO plan C (100mls/kg Ringers Lactate (RL) with intravenous rehydration (IV) given over 3-6 hours according to age including boluses for shock), slow rehydration (100 mls/kg RL over 8 hours (no boluses)) or WHO SAM rehydration regime (ORS only (boluses for shock (standard of care)). Stratum B incorporates all children with moderate dehydration and severe dehydration post-intravenous rehydration and compares (1:1 ratio) standard WHO ORS given for non-SAM (experimental) versus WHO SAM-recommended low-sodium ReSoMal. The primary outcome for intravenous rehydration is mortality to 96 hours and for oral rehydration a change in sodium levels at 24 hours post-randomisation. Secondary outcomes include measures assessing safety (evidence of pulmonary oedema or heart failure); change in sodium from post-iv levels for those in Stratum A; perturbations of electrolyte abnormalities (severe hyponatraemia <125 mmols/L or hypokalaemia.
If the trial shows that rehydration strategies for non-malnourished children are safe and improve mortality in SAM this could prompt revisions to the current treatment recommendations or may prompt future Phase III trials.
因重度急性营养不良(SAM)住院的儿童常并发腹泻(≥3次水样便/天)(发生率>50%),且预后较差。基于专家意见,SAM的补液指南极为保守且存在争议。该指南仅允许在出现重度休克的情况下使用静脉补液,且因担心液体和/或钠超载,仅允许使用低钠静脉补液和口服补液盐(ORS)。按照这些指南进行治疗的儿童死亡率极高。拟开展的GASTROSAM试验将以死亡率作为主要结局,重新评估当前的建议。我们假设,对于患有腹泻的SAM儿童,采用更为宽松的静脉和口服补液策略可能会减少不良结局。
一项开放的II期试验,采用部分析因设计,纳入乌干达、肯尼亚、尼日利亚和尼日尔年龄在6个月至12岁、因肠胃炎(>3次稀便/天)住院且有中度和重度脱水体征的SAM儿童。在A组(重度脱水),儿童将被随机分配(1:1:2)至世界卫生组织(WHO)方案C(100毫升/千克乳酸林格液(RL),根据年龄在3 - 6小时内进行静脉补液(IV),包括用于休克的推注量)、缓慢补液(100毫升/千克RL在8小时内(无推注量))或WHO的SAM补液方案(仅ORS(用于休克的推注量(标准治疗)))。B组纳入所有中度脱水以及静脉补液后仍为重度脱水的儿童,并比较(1:1比例)针对非SAM的标准WHO ORS(试验组)与WHO推荐的低钠ReSoMal。静脉补液的主要结局是96小时内的死亡率,口服补液的主要结局是随机分组后24小时钠水平的变化。次要结局包括评估安全性的指标(肺水肿或心力衰竭的证据);A组儿童静脉补液后钠水平的变化;电解质异常的扰动(严重低钠血症<125毫摩尔/升或低钾血症)。
如果试验表明非营养不良儿童的补液策略安全且能提高SAM儿童的死亡率,这可能促使对当前治疗建议进行修订,或促使未来开展III期试验。